450 results on '"Zakharova, Ekaterina"'
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2. Ac-DEVD-CHO (caspase-3/DEVDase inhibitor) suppresses self-incompatibility–induced programmed cell death in the pollen tubes of petunia (Petunia hybrida E. Vilm.)
3. Demo: Model of Distributed Sorting System with Robotic Agents.
4. Smart Transport as an Enhancement of the Urban Infrastructure
5. Smart Transport as an Enhancement of the Urban Infrastructure
6. A New Case of Mitochondrial RNA Helicase SUPV3L1-Associated Neurodegenerative Disease: Ataxia, Spasticity, Optic Atrophy, and Skin Hypopigmentation (ASOASH).
7. Additive effect of frequent polymorphism and rare synonymous variant alters splicing in twin patients with Niemann-Pick disease type C
8. Publisher Correction: Processed pseudogene insertion in GLB1 causes Morquio B disease by altering intronic splicing regulatory landscape
9. Processed pseudogene insertion in GLB1 causes Morquio B disease by altering intronic splicing regulatory landscape
10. Identification of a Novel Indel Variant in the DARS2 Gene in Russian Patients with Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation
11. New Case of Spinocerebellar Ataxia, Autosomal Recessive 4, Due to VPS13D Variants
12. Alkaptonuria in Russia: mutational spectrum and novel variants
13. Retrospective analysis of 17 patients with mitochondrial membrane protein-associated neurodegeneration diagnosed in Russia
14. POLG-associated ataxias can represent a substantial part of recessive and sporadic ataxias in adults
15. Genetic landscape of pediatric acute liver failure of indeterminate origin
16. Caspase-like proteases and the phytohormone cytokinin as determinants of S-RNAse–based self-incompatibility–induced PCD in Petunia hybrida L.
17. Structural Parameters of the Brain and Bone Structures of the Head and Neck in Patients with Various Types of Mucopolysaccharidoses According to Magnetic Resonance Imaging of the Brain
18. The Effect of p.G2019S Mutation in the LRRK2 Gene on the Activity of Lysosomal Hydrolases and the Clinical Features of Parkinson's Disease Associated with p.N370S Mutation in the GBA1 Gene
19. Molecular and biochemical study of glutaric aciduria type 1 in 49 Russian families: nine novel mutations in the GCDH gene
20. Analysis of long-term observations of the large group of Russian patients with Hunter syndrome (mucopolysaccharidosis type II)
21. Phylogeny and taxonomic review of Oreocomopsis with description of a new genus Oreocomoides (Apioideae, Apiaceae)
22. The Role of Reactive Oxygen Species in the In Vitro Germination and Growth of the Petunia (Petunia hybrida E. Vilm.) Male Gametophyte
23. Genetic landscape of pediatric acute liver failure of indeterminate origin
24. Generation of induced pluripotent stem cell line (RCMGi012-A) from fibroblasts of patient with mucopolysaccharidosis type VI
25. TOPKAR - A GEOGRAPHIC INFORMATION SYSTEM FOR TOPONYMS OF KARELIA: HISTORICAL AND GEOGRAPHICAL ASPECT
26. Pediatric Patients with Sitosterolemia: Next-Generation Sequencing and Biochemical Examination in Clinical Practice
27. Infrageneric classification of Elwendia (Apiaceae) with a restored species
28. Mysterious masks of hypercholesterolemia: A very rare clinical case
29. What is Seseli diffusum? A comparative morphological and molecular appraisal of a critical species of the Umbelliferae
30. Four Novel Disease-Causing Variants in the NOTCH3 Gene in Russian Patients with CADASIL
31. New Acylcarnitine Ratio as a Reliable Indicator of Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency
32. Modern Approaches to the Management of Children with Hypophosphatasia
33. Sorting Space Configuration Comparison for the Multi-Agent Robotic Sorting System*
34. Whole Transcriptome Analysis of Substantia Nigra in Mice with MPTP-Induced Parkinsonism Bearing Defective Glucocerebrosidase Activity
35. Clinical Characterization of Alagille Syndrome in Patients with Cholestatic Liver Disease
36. Hormonal Signaling during dPCD: Cytokinin as the Determinant of RNase-Based Self-Incompatibility in Solanaceae
37. Potential Binding Sites of Pharmacological Chaperone NCGC00241607 on Mutant β-Glucocerebrosidase and Its Efficacy on Patient-Derived Cell Cultures in Gaucher and Parkinson’s Disease
38. Clinical and Genetic Characteristics of Calvarial Doughnut Lesions with Bone Fragility in Three Families with a Reccurent SGMS2 Gene Variant
39. Genetic Variability of HUPRA Syndrome—A Case Report
40. The Study of Crystals in the Fruits of Some Apiaceae Species Using Energy-Dispersive Spectroscopy
41. Elwendia Boissier 1844
42. Elwendia (sect. Elwendia) sect. Elwendia
43. Oxysterol/chitotriosidase based selective screening for Niemann-Pick type C in infantile cholestasis syndrome patients
44. Chronic visceral acid sphingomyelinase deficiency (Niemann-Pick disease type B) in 16 Polish patients: long-term follow-up
45. Toward the Synthesis of Heteroleptic Zinc ROP Initiators Based on Pyridine-Containing Monoalcohols by Tuning Ligand Substituents
46. Association of rare variants inARSAwith Parkinson’s disease
47. Development of and research into a rigid algorithm for analyzing Twitter publications and its influence on the movements of the cryptocurrency market
48. Results of 14-year-long Enzyme Replacement Therapy in a Patient with Mucopolysaccharidosis Type II: Clinical Case
49. Alfa-mannosidosis: Frequent Symptoms in Rare Patient
50. How to Distinguish Attenuated Forms of Mucopolysaccharidosis and Articular Forms of Juvenile Arthritis: Development of Diagnostic Algorithm Based on the Data from Multicenter Retrospective Study
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